N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

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N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

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N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

@nl

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Item

label

N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

@en

N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

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N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

@en

N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

@nl

P1476

N-Heterocyclic carbene-catalyzed sulfa-Michael addition of enals.

@en

P2093

Bin Dai

http://www.w3.org/2001/XMLSchema#string

Cheng-Zhi Gu

http://www.w3.org/2001/XMLSchema#string

Guang-Fen Du

http://www.w3.org/2001/XMLSchema#string

Lin He

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Yang-Guo Li

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Zi-Song Cong

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P2860

Mechanistic, crystallographic, and computational studies on the catalytic, enantioselective sulfenofunctionalization of alkenes.

Organocatalytic Reactions Enabled by N-Heterocyclic Carbenes

Asymmetric multicomponent domino reactions and highly enantioselective conjugated addition of thiols to alpha,beta-unsaturated aldehydes

An overview of N-heterocyclic carbenes

Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters

α,β-Unsaturated acyl azoliums from N-heterocyclic carbene catalyzed reactions: observation and mechanistic investigation.

Enantioselective β-Protonation by a Cooperative Catalysis Strategy.

Organocatalysis by N-heterocyclic carbenes.

A dual Lewis base activation strategy for enantioselective carbene-catalyzed annulations.

Catalytic asymmetric conjugate addition of simple alkyl thiols to alpha,beta-unsaturated N-acylated oxazolidin-2-ones with bifunctional catalysts.

P304

13129-13132

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P31

scholarly article

P356

10.1039/C7CC07269D

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-11-22T00:00:00Z

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P698

29164194

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